Li Shuo Hao, Liu Xu, Hu Weigang, Chen Mingyang, Zhu Yan
School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, P. R. China.
Center for Green Innovation, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083, P. R. China.
J Phys Chem A. 2020 Jul 23;124(29):6061-6067. doi: 10.1021/acs.jpca.0c03366. Epub 2020 Jul 8.
Atomically precise metal clusters are now in the research spotlight, owing to the precise correlation between the physicochemical properties and their atomic-packing structures at an atomic-level. Herein we synthesized an Au cluster capped by four ferrocene ligands (DPPF), in which the ferrocene not only can direct the precise formation of the Au cluster, but also can solidify the structural pattern of the Au cluster. The Au(DPPF) clusters as heterogeneous catalysts can achieve efficiently catalytic performances for the CO oxidation reaction, mainly due to the resistance to aggregation into large particles under reaction conditions. Our results suggest that the homolytic phosphine dissociation nature and the postdissociation reconstruction effect induced by Fe may enhance the catalytic performances of Au(DPPF).
由于在原子水平上物理化学性质与其原子堆积结构之间存在精确的相关性,原子精确的金属簇目前正处于研究的热点。在此,我们合成了一种由四个二茂铁配体(DPPF)封端的金簇,其中二茂铁不仅可以指导金簇的精确形成,还可以固化金簇的结构模式。作为多相催化剂的Au(DPPF)簇对于CO氧化反应可以实现高效的催化性能,这主要是由于在反应条件下其抗聚集形成大颗粒的能力。我们的结果表明,均裂膦解离性质以及由铁诱导的解离后重构效应可能会提高Au(DPPF)的催化性能。